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Detail of "13393-93-6"

  • CAS Number:
  • 13393-93-6
  • Name:
  • 1-Phenanthrenemethanol,tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R,4aR,4bS,10aR)-

  • Molecular Structure:
  • Formula:
  • C20H36 O
  • Molecular Weight:
  • 292.5
  • Synonyms:
  • 1-Phenanthrenemethanol,tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-; Abietyl alcohol, tetrahydro-(6CI); Tetrahydroabietyl alcohol
  • EINECS:
  • 236-476-3
  • Density:
  • 0.93 g/cm3
  • Boiling Point:
  • 375.5 °C at 760 mmHg
  • Flash Point:
  • 175.8 °C

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CAS No.13393-93-6 ABITOL

ABITOL

Supplier:TECHLAB SA [ France]

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Tel:(33) 03 87 75 54 29

Address:France

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CAS No.13393-93-6 ABITOL

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Supplier:J.H. Calo Company, Inc. [ United States]

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Tel:866 300 3256

Address:1600 Stewart Ave. Suite 303, Westbury, NY 11590

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CAS No.13393-93-6 1-Phenanthrenemethanol,tetradecahydro-1,4a-dimethyl-7-(1-methylethyl)-, (1R,4aR,4bS,10aR)-

Supplier:AccuStandard Inc [ United States]

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Tel:(800) 442-5290

Address:AccuStandard Inc

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Reference

Monographs on fragrance raw materials
Monographs on fragrance raw materials. Hydroabietyl alcohol. Opdyke, D. L. J. (Res. Inst. Fragrance Mater., Inc., Englewood Cliffs, N. J., USA). Food Cosmet. Toxicol. 13393-93-6 is the cas registry number of certain chemical which is used as reagents here., 12, Suppl., 919-20 (English) 1974. CODEN: FCTXAV. DOCUMENT TYPE: Journal; General Review CA Section: 62 (Essential Oils and Cosmetics) The prepn., phys. properties, cosmetic and perfume uses, legal status of use in food, and toxicol. of hydroabietyl alc. (I) [13393-93-6] are reviewed with 7 refs. .
Components of Labiatae
Components of Labiatae. XXV. Diterpenes from Nepeta granatensis Boiss. Chromic oxidation of the allylic alcohols 7.alpha.,18-dihydroxy-14-abietene and 14.alpha.,18-dihydroxy-7-abietene. Gonzalez Gonzalez, Antonio; Breton, J. L.; Fagundo, C. R.; Trujillo, J. M. (Dep. Quim. Org., Univ. La Laguna, La Laguna, Spain). An. Quim., 72(1), 65-70 (Spanish) 1976. CODEN: ANQUBU. DOCUMENT TYPE: Journal CA Section: 30 (Terpenoids) Alcs. isolated from N. granatensis were identified as 7.alpha.,18-dihydroxy-14-abietene (I) and 14.alpha.,18-dihydroxy-7-abietene (II) by their chem. reactions. 13393-93-6 and 61866-62-4 are just another two chemicals used in this study. CrO3 oxidn. of I and II gave the epoxy ketone III. II was also hydrogenated and oxidized to 14-oxo-18-abietanoic acid or oxidized to the 14-oxo compd. .
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